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Stefan Vielhaber (1965-)

Neurologe

Name	Stefan Vielhaber
Zeit	1965- (Lebensdaten)
Ort	Aachen (Wirkungsort) Sundern (Sauerland) (Geburtsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Neurologe (charakteristischer Beruf) Arzt
Variante	Stephan Vielhaber Stefan Antonius Vielhaber Stefan A. Vielhaber
Beziehung	Universitätsklinikum Magdeburg
Datensatztyp	Person
GND-Nummer	172770475
Datensatz-ID	172770475
Beteiligt an alle anzeigen A systematic review of progranulin concentrations in biofluids in over 7,000 people—assessing the pathogenicity of GRN mutations and other influencing factors Cytokine alterations in CSF and serum samples of patients with a first episode of schizophrenia: results and methodological considerations The brain reacting to COVID-19: analysis of the cerebrospinal fluid proteome, RNA and inflammation Classifying flow cytometry data using Bayesian analysis helps to distinguish ALS patients from healthy controls Peripheral Nerve Ultrasound for the Differentiation between ALS, Inflammatory, and Hereditary Polyneuropathies Counteraction of inflammatory activity in CAA-related subarachnoid hemorrhage Small fiber involvement is independent from clinical pain in late-onset Pompe disease Independent risk factors for myasthenic crisis and disease exacerbation in a retrospective cohort of myasthenia gravis patients Counteraction of inflammatory activity in CAA-related subarachnoid hemorrhage Die Implantation von Carmustin Wafern zur Therapie des rezidivierenden Glioblastoms im klinischen Alltag Eculizumab versus rituximab in generalised myasthenia gravis Independent risk factors for myasthenic crisis and disease exacerbation in a retrospective cohort of myasthenia gravis patients Zerebrale Mikroblutungen in der 7 Tesla-Magnetresonanztomographie : Eine QSM-Studie Amyotrophic lateral sclerosis patients show increased peripheral and intrathecal T-cell activation Messung des Nervenwasserdurchflusses mittels Phasenkontrastmagnetresonanztomographie in ventrikuloperitonealen Ableitungen mit magnetisch verstellbaren Ventilen The ARCA registry: a collaborative global platform for advancing trial readiness in autosomal recessive cerebellar ataxias 7T MR neurography-ultrasound fusion for peripheral nerve imaging Laryngopharyngeale Symptome der Multisystematrophie : Möglichkeiten zur Verbesserung der Diagnose Stellenwert der Dekompressionskraniektomie bei aneurysmatisch bedingter Subarachnoidalblutung Textural markers of ultrasonographic nerve alterations in amyotrophic lateral sclerosis The upper cervical spinal cord in ALS assessed by cross-sectional and longitudinal 3T MRI The Dyspnea-ALS-Scale (DALS-15) optimizes individual treatment in patients with amyotrophic lateral sclerosis (ALS) suffering from dyspnea An integrative correlation of myopathology, phenotype and genotype in late onset Pompe disease Retrospektive Datenanalyse von 32 Patienten mit Myositis Significance of CSF NfL and tau in ALS Rhinocerebrale Mucormykose Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia Das Verhalten von Restingstate-Networks bei Amyotropher Lateralsclerose : eine Analyse an Subgruppen von an ALS-erkrankten Patienten im Vergleich zu gesunden Kontrollen Working Memory Network Changes in ALS Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study Longitudinal course of cortical thickness decline in amyotrophic lateral sclerosis Memory deficits in amyotrophic lateral sclerosis are not exclusively caused by executive dysfunction: a comparative neuropsychological study of amnestic mild cognitive impairment Transkranielle Magnetstimulation (TKMS) und somatosensibel evozierte Potentiale (SEP) bei kernspintomographisch gesicherten Hirnstamminfarkten

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Katalog der Deutschen Nationalbibliothek

Stefan Vielhaber (1965-)

A systematic review of progranulin concentrations in biofluids in over 7,000 people—assessing the pathogenicity of GRN mutations and other influencing factors

Cytokine alterations in CSF and serum samples of patients with a first episode of schizophrenia: results and methodological considerations

The brain reacting to COVID-19: analysis of the cerebrospinal fluid proteome, RNA and inflammation

Classifying flow cytometry data using Bayesian analysis helps to distinguish ALS patients from healthy controls

Peripheral Nerve Ultrasound for the Differentiation between ALS, Inflammatory, and Hereditary Polyneuropathies

Counteraction of inflammatory activity in CAA-related subarachnoid hemorrhage

Small fiber involvement is independent from clinical pain in late-onset Pompe disease

Independent risk factors for myasthenic crisis and disease exacerbation in a retrospective cohort of myasthenia gravis patients

Counteraction of inflammatory activity in CAA-related subarachnoid hemorrhage

Die Implantation von Carmustin Wafern zur Therapie des rezidivierenden Glioblastoms im klinischen Alltag

Eculizumab versus rituximab in generalised myasthenia gravis

Independent risk factors for myasthenic crisis and disease exacerbation in a retrospective cohort of myasthenia gravis patients

Zerebrale Mikroblutungen in der 7 Tesla-Magnetresonanztomographie : Eine QSM-Studie

Amyotrophic lateral sclerosis patients show increased peripheral and intrathecal T-cell activation

Messung des Nervenwasserdurchflusses mittels Phasenkontrastmagnetresonanztomographie in ventrikuloperitonealen Ableitungen mit magnetisch verstellbaren Ventilen

The ARCA registry: a collaborative global platform for advancing trial readiness in autosomal recessive cerebellar ataxias

7T MR neurography-ultrasound fusion for peripheral nerve imaging

Laryngopharyngeale Symptome der Multisystematrophie : Möglichkeiten zur Verbesserung der Diagnose

Stellenwert der Dekompressionskraniektomie bei aneurysmatisch bedingter Subarachnoidalblutung

Textural markers of ultrasonographic nerve alterations in amyotrophic lateral sclerosis

The upper cervical spinal cord in ALS assessed by cross-sectional and longitudinal 3T MRI

The Dyspnea-ALS-Scale (DALS-15) optimizes individual treatment in patients with amyotrophic lateral sclerosis (ALS) suffering from dyspnea

An integrative correlation of myopathology, phenotype and genotype in late onset Pompe disease

Retrospektive Datenanalyse von 32 Patienten mit Myositis

Significance of CSF NfL and tau in ALS

Rhinocerebrale Mucormykose

Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia

Das Verhalten von Restingstate-Networks bei Amyotropher Lateralsclerose : eine Analyse an Subgruppen von an ALS-erkrankten Patienten im Vergleich zu gesunden Kontrollen

Working Memory Network Changes in ALS

Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study

Longitudinal course of cortical thickness decline in amyotrophic lateral sclerosis

Memory deficits in amyotrophic lateral sclerosis are not exclusively caused by executive dysfunction: a comparative neuropsychological study of amnestic mild cognitive impairment

Transkranielle Magnetstimulation (TKMS) und somatosensibel evozierte Potentiale (SEP) bei kernspintomographisch gesicherten Hirnstamminfarkten